Single‐Atom Engineering for Synergistic Nucleation and Interfacial Regulation Enabling Durable Anode‐Free Sodium Metal Batteries

S Shenghui Zhou Z Zhefei Sun (State Key Laboratory of Physical Chemistry of Solid Surfaces, College of Materials) J Jiaming Zhang (College of Energy Materials and Chemistry, College of Chemistry and Chemical Engineering) H Huiping Yang Z Zhiyi Sun Q Qing Zhang S Sifan Wen (State Key Laboratory of Physical Chemistry of Solid Surfaces College of Materials Xiamen University Xiamen 361005 China) H Haoyu Chen Q Quanzhi Yin (State Key Laboratory of Physical Chemistry of Solid Surfaces College of Materials Xiamen University Xiamen 361005 China) S Shijie Feng J Jiajia Han (Department of Materials Science and Engineering, College of Materials) L Lin Zeng (Shenzhen Key Laboratory of Advanced Energy Storage, Department of Mechanical and Energy Engineering) W Wenxing Chen (School of Materials Science and Engineering) J Jie Li L Li Zhang D Dong‐Liang Peng (State Key Laboratory of Physical Chemistry of Solid Surfaces Fujian Key Laboratory of Surface and Interface Engineering for High Performance Materials College of Materials Xiamen University Xiamen P. R. China) Q Qiaobao Zhang (State Key Laboratory of Physical Chemistry of Solid Surfaces, College of Materials)

Abstract

Abstract Anode‐free sodium metal batteries (AFSMBs) are highly promising candidates for low‐cost, sustainable, and high‐energy‐density storage systems. However, their practical deployment is challenged by uncontrolled dendrite growth and unstable solid electrolyte interphase (SEI) formation. To address these issues, a highly reversible and robust Na metal host enabled by atomic Bi sites is devised, coordinated in a unique N 3 ‐Bi‐S 1 moiety anchored on interconnected carbon tubes (Bi‐N 3 S 1 @CT). Crucially, this designed remarkably sodiophilic Bi single‐atom promotes uniform Na nucleation with minimal Na + consumption, enabling durable and highly reversible Na plating/stripping, while effectively suppressing electrolyte over‐decomposition and fostering the formation of robust inorganic‐rich SEI films, as supported by comprehensive theoretical calculations and experimental analyses. Consequently, Bi‐N 3 S 1 @CT achieves an extraordinary average Coulombic efficiency (CE) of 99.6% over 900 cycles at 12 mA cm −2 and 6 mAh cm −2 , along with long‐term durability of 1000 h at 10 mA cm −2 and 10 mAh cm −2 in symmetric cells. Notably, an anode‐free pouch cell paired with a high‐loading Na 3 V 2 (PO 4 ) 3 cathode exhibits decent cyclability over 240 cycles at 1C while maintaining good rate capability. This work demonstrates a promising strategy to simultaneously enhance energy density and stability in AFSMBs via atomic‐level sodiophilicity regulation and SEI engineering.

Article Details

Volume / Issue Vol. 38, Issue 7
Published February 01, 2026
ISSN 0935-9648
Publisher Unknown Publisher

Journal Info

Advanced Materials

Unknown Publisher

ISSN: 0935-9648 Physical Sciences

Authors (17)

S

Shenghui Zhou

Z

Zhefei Sun

State Key Laboratory of Physical Chemistry of Solid Surfaces, College of Materials

J

Jiaming Zhang

College of Energy Materials and Chemistry, College of Chemistry and Chemical Engineering

H

Huiping Yang

Z

Zhiyi Sun

Q

Qing Zhang

S

Sifan Wen

State Key Laboratory of Physical Chemistry of Solid Surfaces College of Materials Xiamen University Xiamen 361005 China

H

Haoyu Chen

Q

Quanzhi Yin

State Key Laboratory of Physical Chemistry of Solid Surfaces College of Materials Xiamen University Xiamen 361005 China

S

Shijie Feng

J

Jiajia Han

Department of Materials Science and Engineering, College of Materials

L

Lin Zeng

Shenzhen Key Laboratory of Advanced Energy Storage, Department of Mechanical and Energy Engineering

W

Wenxing Chen

School of Materials Science and Engineering

J

Jie Li

L

Li Zhang

D

Dong‐Liang Peng

State Key Laboratory of Physical Chemistry of Solid Surfaces Fujian Key Laboratory of Surface and Interface Engineering for High Performance Materials College of Materials Xiamen University Xiamen P. R. China

Q

Qiaobao Zhang

State Key Laboratory of Physical Chemistry of Solid Surfaces, College of Materials